Canonical Allele Identifier: CA364951875
Gene: GABRR1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.89217254T>G , CM000668.2:g.89217254T>G GRCh38
NC_000006.11:g.89926973T>G , CM000668.1:g.89926973T>G GRCh37
NC_000006.10:g.89983692T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000454853.7:c.69A>C MANE Select ENSP00000412673.2:p.Glu23Asp
ENST00000369451.7:c.-239+4021A>C ENSP00000358463.3:n.-239+4021A>C
ENST00000435811.5:c.69A>C ENSP00000394687.1:p.Glu23Asp
ENST00000454853.6:c.69A>C ENSP00000412673.2:p.Glu23Asp
ENST00000457434.1:c.69A>C ENSP00000410130.1:p.Glu23Asp
ENST00000481493.1:n.8A>C
ENST00000611484.4:c.-295A>C ENSP00000478846.1:n.-295A>C
ENST00000621627.4:c.-242+4021A>C ENSP00000481986.1:n.-242+4021A>C
NM_001256703.1:c.69A>C NP_001243632.1:p.Glu23Asp
NM_001256704.1:c.-295A>C NP_001243633.1:n.-295A>C
NM_001267582.1:c.-242+4021A>C NP_001254511.1:n.-242+4021A>C
NM_002042.4:c.69A>C NP_002033.2:p.Glu23Asp
XM_006715438.2:c.69A>C XP_006715501.1:p.Glu23Asp
XM_017010689.1:c.-292A>C XP_016866178.1:n.-292A>C
NM_002042.5:c.69A>C MANE Select NP_002033.2:p.Glu23Asp
NM_001267582.2:c.-242+4021A>C NP_001254511.1:n.-242+4021A>C